Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

C/T | Ancestral: C | Ambiguity code: Y

Chromosome 16:23603525 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


This variant has 2 synonyms - Show

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 5 transcripts, is associated with 2 phenotypes and is mentioned in 3 citations.

Variant displays